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Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing
We present a systematic assessment of RainDrop BS-seq, a novel method for large-scale, targeted bisulfite sequencing using microdroplet-based PCR amplification coupled with next-generation sequencing. We compared DNA methylation levels at 498 target loci (1001 PCR amplicons) in human whole blood, os...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Landes Bioscience
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063826/ https://www.ncbi.nlm.nih.gov/pubmed/24518816 http://dx.doi.org/10.4161/epi.28041 |
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author | Paul, Dirk S Guilhamon, Paul Karpathakis, Anna Butcher, Lee M Thirlwell, Christina Feber, Andrew Beck, Stephan |
author_facet | Paul, Dirk S Guilhamon, Paul Karpathakis, Anna Butcher, Lee M Thirlwell, Christina Feber, Andrew Beck, Stephan |
author_sort | Paul, Dirk S |
collection | PubMed |
description | We present a systematic assessment of RainDrop BS-seq, a novel method for large-scale, targeted bisulfite sequencing using microdroplet-based PCR amplification coupled with next-generation sequencing. We compared DNA methylation levels at 498 target loci (1001 PCR amplicons) in human whole blood, osteosarcoma cells and an archived tumor tissue sample. We assessed the ability of RainDrop BS-seq to accurately measure DNA methylation over a range of DNA quantities (from 10 to 1500 ng), both with and without whole-genome amplification (WGA) following bisulfite conversion. DNA methylation profiles generated using at least 100 ng correlated well (median R = 0.92) with those generated on Illumina Infinium HumanMethylation450 BeadChips, currently the platform of choice for epigenome-wide association studies (EWAS). WGA allowed for testing of samples with a starting DNA amount of 10 and 50 ng, although a reduced correlation was observed (median R = 0.79). We conclude that RainDrop BS-seq is suitable for measuring DNA methylation levels using nanogram quantities of DNA, and can be used to study candidate epigenetic biomarker loci in an accurate and high-throughput manner, paving the way for its application to routine clinical diagnostics. |
format | Online Article Text |
id | pubmed-4063826 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | Landes Bioscience |
record_format | MEDLINE/PubMed |
spelling | pubmed-40638262015-05-01 Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing Paul, Dirk S Guilhamon, Paul Karpathakis, Anna Butcher, Lee M Thirlwell, Christina Feber, Andrew Beck, Stephan Epigenetics Brief Report We present a systematic assessment of RainDrop BS-seq, a novel method for large-scale, targeted bisulfite sequencing using microdroplet-based PCR amplification coupled with next-generation sequencing. We compared DNA methylation levels at 498 target loci (1001 PCR amplicons) in human whole blood, osteosarcoma cells and an archived tumor tissue sample. We assessed the ability of RainDrop BS-seq to accurately measure DNA methylation over a range of DNA quantities (from 10 to 1500 ng), both with and without whole-genome amplification (WGA) following bisulfite conversion. DNA methylation profiles generated using at least 100 ng correlated well (median R = 0.92) with those generated on Illumina Infinium HumanMethylation450 BeadChips, currently the platform of choice for epigenome-wide association studies (EWAS). WGA allowed for testing of samples with a starting DNA amount of 10 and 50 ng, although a reduced correlation was observed (median R = 0.79). We conclude that RainDrop BS-seq is suitable for measuring DNA methylation levels using nanogram quantities of DNA, and can be used to study candidate epigenetic biomarker loci in an accurate and high-throughput manner, paving the way for its application to routine clinical diagnostics. Landes Bioscience 2014-05-01 2014-02-11 /pmc/articles/PMC4063826/ /pubmed/24518816 http://dx.doi.org/10.4161/epi.28041 Text en Copyright © 2014 Landes Bioscience http://creativecommons.org/licenses/by/3.0/ This is an open-access article licensed under a Creative Commons Attribution 3.0 Unported License. The article may be redistributed, reproduced, and reused for non-commercial purposes, provided the original source is properly cited. |
spellingShingle | Brief Report Paul, Dirk S Guilhamon, Paul Karpathakis, Anna Butcher, Lee M Thirlwell, Christina Feber, Andrew Beck, Stephan Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing |
title | Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing |
title_full | Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing |
title_fullStr | Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing |
title_full_unstemmed | Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing |
title_short | Assessment of RainDrop BS-seq as a method for large-scale, targeted bisulfite sequencing |
title_sort | assessment of raindrop bs-seq as a method for large-scale, targeted bisulfite sequencing |
topic | Brief Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4063826/ https://www.ncbi.nlm.nih.gov/pubmed/24518816 http://dx.doi.org/10.4161/epi.28041 |
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